US5575891A - Soft tissue paper containing an oil and a polyhydroxy compound - Google Patents

Soft tissue paper containing an oil and a polyhydroxy compound Download PDF

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Publication number
US5575891A
US5575891A US08/381,250 US38125095A US5575891A US 5575891 A US5575891 A US 5575891A US 38125095 A US38125095 A US 38125095A US 5575891 A US5575891 A US 5575891A
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United States
Prior art keywords
tissue paper
web
oil
paper
polyhydroxy compound
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US08/381,250
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English (en)
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Paul D. Trokhan
Dean Van Phan
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Procter and Gamble Co
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Procter and Gamble Co
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Application filed by Procter and Gamble Co filed Critical Procter and Gamble Co
Priority to US08/381,250 priority Critical patent/US5575891A/en
Priority to AT96905250T priority patent/ATE193349T1/de
Priority to CA002208643A priority patent/CA2208643C/en
Priority to CN96191681A priority patent/CN1075576C/zh
Priority to DE69608542T priority patent/DE69608542T3/de
Priority to AU49059/96A priority patent/AU713070B2/en
Priority to BR9607084A priority patent/BR9607084A/pt
Priority to PCT/US1996/001145 priority patent/WO1996024719A2/en
Priority to KR1019970705182A priority patent/KR100249609B1/ko
Priority to EP96905250A priority patent/EP0807194B2/en
Priority to JP52429596A priority patent/JP3939345B2/ja
Priority to ES96905250T priority patent/ES2145998T3/es
Priority to ZA96700A priority patent/ZA96700B/xx
Priority to TW085101212A priority patent/TW402653B/zh
Assigned to PROCTER & GAMBLE COMPANY, THE reassignment PROCTER & GAMBLE COMPANY, THE ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: TROKHAN, PAUL DENNIS, VAN PHAN, DEAN
Publication of US5575891A publication Critical patent/US5575891A/en
Application granted granted Critical
Priority to MXPA/A/1997/005778A priority patent/MXPA97005778A/xx
Priority to HK98103946A priority patent/HK1004681A1/xx
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H27/00—Special paper not otherwise provided for, e.g. made by multi-step processes
    • D21H27/002—Tissue paper; Absorbent paper
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/03—Non-macromolecular organic compounds
    • D21H17/04—Hydrocarbons
    • A—HUMAN NECESSITIES
    • A47—FURNITURE; DOMESTIC ARTICLES OR APPLIANCES; COFFEE MILLS; SPICE MILLS; SUCTION CLEANERS IN GENERAL
    • A47K—SANITARY EQUIPMENT NOT OTHERWISE PROVIDED FOR; TOILET ACCESSORIES
    • A47K10/00—Body-drying implements; Toilet paper; Holders therefor
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/03—Non-macromolecular organic compounds
    • D21H17/05—Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
    • D21H17/06—Alcohols; Phenols; Ethers; Aldehydes; Ketones; Acetals; Ketals
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/20—Macromolecular organic compounds
    • D21H17/33—Synthetic macromolecular compounds
    • D21H17/34—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D21H17/36—Polyalkenyalcohols; Polyalkenylethers; Polyalkenylesters
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/20—Macromolecular organic compounds
    • D21H17/33—Synthetic macromolecular compounds
    • D21H17/46—Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D21H17/59—Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/71—Mixtures of material ; Pulp or paper comprising several different materials not incorporated by special processes
    • D21H17/72—Mixtures of material ; Pulp or paper comprising several different materials not incorporated by special processes of organic material
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
    • D21H21/14—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by function or properties in or on the paper
    • D21H21/22—Agents rendering paper porous, absorbent or bulky
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H23/00—Processes or apparatus for adding material to the pulp or to the paper
    • D21H23/02—Processes or apparatus for adding material to the pulp or to the paper characterised by the manner in which substances are added
    • D21H23/22—Addition to the formed paper
    • D21H23/24—Addition to the formed paper during paper manufacture
    • D21H23/26—Addition to the formed paper during paper manufacture by selecting point of addition or moisture content of the paper
    • D21H23/28—Addition before the dryer section, e.g. at the wet end or press section

Definitions

  • This application relates to tissue papers, in particular pattern densified tissue papers, having an enhanced tactile sense of softness.
  • This application particularly relates to tissue papers treated with certain oils and water-soluble polyhydroxy compounds.
  • Paper webs or sheets sometimes called tissue or paper tissue webs or sheets, find extensive use in modern society. These include such staple items as paper towels, facial tissues and sanitary (or toilet) tissues. These paper products can have various desirable properties, including wet and dry tensile strength, absorbency for aqueous fluids (e.g., wettability), low lint properties, desirable bulk, and softness. The particular challenge in papermaking has been to appropriately balance these various properties to provide superior tissue paper.
  • Softness is the tactile sensation perceived by the consumer who holds a particular paper product, rubs it across the skin, and crumples it within the hand.
  • Such tactile perceivable softness can be characterized by, but is not limited to, friction, flexibility, and smoothness, as well as subjective descriptors, such as a feeling like velvet, silk or flannel.
  • This tactile sensation is a combination of several physical properties, including the flexibility or stiffness of the sheet of paper, as well as the texture of the surface of the paper and the frictional properties of the sheet of paper.
  • Stiffness of paper is typically affected by efforts to increase the dry and/or wet tensile strength of the web.
  • Increases in dry tensile strength can be achieved either by mechanical processes to insure adequate formation of hydrogen bonding between the hydroxyl groups of adjacent papermaking fibers, or by the inclusion of certain dry strength additives.
  • Wet strength is typically enhanced by the inclusion of certain wet strength resins, that, being typically cationic, are easily deposited on and retained by the anionic carboxyl groups of the papermaking fibers.
  • the use of both mechanical and chemical means to improve dry and wet tensile strength can also result in stiffer, harsher feeling, less soft tissue papers.
  • debonding agents Certain chemical additives, commonly referred to as debonding agents, can be added to papermaking fibers to interfere with the natural fiber-to-fiber bonding that occurs during sheet formation and drying, and thus lead to softer papers.
  • debonding agents are typically cationic and have certain disadvantages associated with their use in softening tissue papers.
  • Some low molecular weight cationic debonding agents can cause excessive irritation upon contact with human skin.
  • Higher molecular weight cationic debonding agents can be more difficult to apply at low levels to tissue paper, and also tend to have undesirable hydrophobic effects on the tissue paper, e.g., result in decreased absorbency and particularly wettability.
  • these cationic debonding agents operate by disrupting interfiber bonding, they can also decrease tensile strength to such an extent that resins, latex, or other dry strength additives can be required to provide acceptable levels of tensile strength.
  • These dry strength additives not only increase the cost of the tissue paper but can also have other, deleterious effects on tissue softness.
  • cationic debonding agents include conventional quaternary ammonium compounds such as the well known dialkyl dimethyl ammonium salts (e.g., ditallow dimethyl ammonium chloride, ditallow dimethyl ammonium methyl sulfate, di(hydrogenated) tallow dimethyl ammonium chloride etc . . . ).
  • dialkyl dimethyl ammonium salts e.g., ditallow dimethyl ammonium chloride, ditallow dimethyl ammonium methyl sulfate, di(hydrogenated) tallow dimethyl ammonium chloride etc . . .
  • these cationic quaternary ammonium compounds soften the paper by interfering with the natural fiber-to-fiber bonding that occurs during sheet formation and drying. In addition to decreasing tensile strength, these quaternary ammonium compounds also tend to have undesirable hydrophobic effects on the tissue paper, e.g., resulting in decreased absorbency and wettability.
  • Pattern densified paper has certain densified areas of relatively high fiber density, as well as relatively low fiber density, high bulk areas.
  • Such high bulk pattern densified papers are typically formed from a partially dried paper web that has densified areas imparted to it by a foraminous fabric having a patterned displacement of knuckles. See, for example, U.S. Pat. No. 3,301,746 (Sanford et al), issued Jan. 31, 1967; U.S. Pat. No. 3,994,771 (Morgan et al), issued Nov. 30, 1976; and U.S. Pat. No. 4,529,480 (Trokhan), issued Jul. 16, 1985.
  • patterned densification processes Besides tensile strength and bulk, another advantage of such patterned densification processes is that ornamental patterns can be imprinted on the tissue paper.
  • an inherent problem of patterned densification processes is that the fabric side of the tissue paper, i.e. the paper surface in contact with the foraminous fabric during papermaking, is sensed as rougher than the side not in contact with the fabric. This is due to the high bulk fields that form, in essence, protrusions outward from the surface of the paper. It is these protrusions that can impart a tactile sensation of roughness.
  • Tissue paper has also been treated with softeners by "dry web” addition methods.
  • One such method involves moving the dry paper across one face of a shaped block of wax-like softener that is then deposited on the paper surface by a rubbing action.
  • softeners include stearate soaps such as zinc stearate, stearic acid esters, stearyl alcohol, polyethylene glycols such as Carbowax, and polyethylene glycol esters of stearic and lauric acids).
  • Another such method involves dipping the dry paper in a solution or emulsion containing the softening agent. See U.S. Pat. No.
  • tissue paper in particular high bulk, pattern densified tissue papers
  • a process that: (1) uses a "wet web” method for adding the softening agent; (2) can be carried out in a commercial papermaking system without significantly impacting on machine operability; (3) uses softeners that are nontoxic; and (4) can be carried out in a manner so as to maintain desirable tensile strength, absorbency and low lint properties of the tissue paper.
  • the present invention provides soft, absorbent tissue paper products.
  • the soft tissue paper products comprise:
  • tissue paper from about 0.01% to about 5% of an oil selected from the group consisting of petroleum-based oils, polysiloxane-based oils, and mixtures thereof, based on the dry fiber weight of said tissue paper;
  • tissue paper has a basis weight of from about 10 to about 65 g/m2 and a density of less than about 0.60 g/cc, said polyhydroxy compound and said oil having being applied to a least one surface of a wet tissue paper web.
  • the present invention further relates to a process for making these softened tissue papers.
  • the process includes the steps:
  • nonionic compounds have high rates of retention even in the absence of cationic retention aids or debonding agents when applied to wet tissue paper webs in accordance with the process disclosed herein. This is especially unexpected because the nonionic oils and polyhdroxy compounds are applied to the wet webs under conditions wherein they are not ionically substantive to the cellulose fibers. Importantly, the wet web process allows the polyhydroxy compounds to migrate to the interior of the paper web where they act to enhance the tissue paper absorbency and softness.
  • Tissue paper softened according to the present invention has a soft feel. It is especially useful in softening high bulk, pattern densified tissue papers, including tissue papers having patterned designs.
  • the present invention can be carried out in a commercial papermaking system without significantly impacting on machine operability, including speed.
  • the improved softness benefits of the present invention can also be achieved while maintaining the desirable tensile strength, absorbency (e.g., wettability), and low lint properties of the paper.
  • FIG. 1 is a schematic representation of one embodiment of a continuous papermaking machine which illustrates the preferred process of the present invention of adding treatment chemicals to a pattern densified tissue paper web.
  • the term “comprising” means that the various components, ingredients, or steps, can be conjointly employed in practicing the present invention. Accordingly, the term “comprising” encompasses the more restrictive terms “consisting essentially of” and “consisting of”.
  • tissue paper web, paper web, web, paper sheet and paper product all refer to sheets of paper made by a process comprising the steps of forming an aqueous papermaking furnish, depositing this furnish on a foraminous surface, such as a Fourdrinier wire, and removing the water from the furnish as by gravity or vacuum-assisted drainage, with or without pressing, and by evaporation.
  • an aqueous papermaking furnish is an aqueous slurry of papermaking fibers and the chemicals described hereinafter.
  • the term “consistency” refers to the weight percentage of the cellulosic paper making fibers (i.e., pulp) in the wet tissue web. It is expressed as a weight percentage of this fibrous material, in the wet web, in terms of air dry fiber weight divided by the weight of the wet web.
  • the first step in the process of this invention is the forming of an aqueous papermaking furnish.
  • the furnish comprises papermaking fibers (hereinafter sometimes referred to as wood pulp). It is anticipated that wood pulp in all its varieties will normally comprise the papermaking fibers used in this invention. However, other cellulose fibrous pulps, such as cotton liners, bagasse, rayon, etc., can be used and none are disclaimed.
  • Wood pulps useful herein include chemical pulps such as Kraft, sulfite and sulfate pulps as well as mechanical pulps including for example, ground wood, thermomechanical pulps and chemically modified thermomechanical pulp (CTMP). Pulps derived from both deciduous and coniferous trees can be used.
  • CMP chemically modified thermomechanical pulp
  • the papermaking fibers used in this invention comprise Kraft pulp derived from northern softwoods.
  • the aqueous papermaking furnish is formed into a wet web on a foraminous forming carrier, such as a Fourdrinier wire, as will be discussed hereinafter.
  • the present invention contains as an essential component from about 0.01% to about 5.0%, preferably from 0.05% to about 2.0%, more preferably from about 0.1% to about 1.0%, of a water soluble polyhydroxy compound, based on the dry fiber weight of the tissue paper.
  • water soluble polyhydroxy compounds suitable for use in the present invention include glycerol, polyglycerols having a weight average molecular weight of from about 150 to about 800 and polyoxyethylene glycol and polyoxypropylene glycol having a weight-average molecular weight of from about 200 to about 4000, preferably from about 200 to about 1000, most preferably from about 200 to about 600.
  • Polyoxyethylene glycol having an weight average molecular weight of from about 200 to about 600 are especially preferred.
  • Mixtures of the above-described polyhydroxy compounds may also be used. For example, mixtures of glycerol and polyglycerols, mixtures of glycerol and polyoxyethylene glycols, mixtures of polyglycerols and polyoxyethylene glycols, etc. .
  • a particularly preferred polyhydroxy compound is polyoxyethylene glycol having an weight average molecular weight of about 400. This material is available commercially from the Union Carbide Company of Danbury, Conn. under the tradename "PEG-400".
  • the present invention contains as an essential component from about 0.01% to about 5.0%, preferably from 0.05% to about 2.0%, more preferably from about 0.1% to about 1.0%, by weight of an oil selected from the group consisting of petroleum-based oils, polysiloxane-based oils, and mixtures thereof, based on the dry fiber weight of the tissue paper.
  • the term petroleum-based oils refers to viscous mixtures of hydrocarbons having from about 16 to about 32 carbon atoms.
  • the petroleum-based oil is a petroleum-based turbine oil comprised primarily of saturated hydrocarbons.
  • An example of a preferred petroleum-based turbine oil for use in the present invention is known as "Regal Oil”.
  • the term "Regal Oil” refers to the compound which is comprised of approximately 87% saturated hydrocarbons and approximately 12.6% aromatic hydrocarbons with traces of additives, manufactured as product number R & O 68 Code 702 by the Texaco Oil Company of Houston, Tex.
  • suitable polysiloxane materials for use in the present invention include those having monomeric siloxane units of the following structure: ##STR1## wherein, R 1 and R 2 , for each independent siloxane monomeric unit can each independently be hydrogen or any alkyl, aryl, alkenyl, alkaryl, arakyl, cycloalkyl, halogenated hydrocarbon, or other radical. Any of such radicals can be substituted or unsubstituted. R 1 and R 2 radicals of any particular monomeric unit may differ from the corresponding functionalities of the next adjoining monomeric unit. Additionally, the polysiloxane can be either a straight chain, a branched chain or have a cyclic structure.
  • the radicals R 1 and R 2 can additionally independently be other silaceous functionalities such as, but not limited to siloxanes, polysiloxanes, silanes, and polysilanes.
  • the radicals R 1 and R 2 may contain any of a variety of organic functionalities including, for example, alcohol, carboxylic acid, aldehyde, ketone and amine, amide functionalities.
  • Exemplary alkyl radicals are methyl, ethyl, propyl, butyl, pentyl, hexyl, octyl, decyl, octadecyl, and the like.
  • Exemplary alkenyl radicals are vinyl, allyl, and the like.
  • Exemplary aryl radicals are phenyl, diphenyl, naphthyl, and the like.
  • Exemplary alkaryl radicals are toyl, xylyl, ethylphenyl, and the like.
  • Exemplary arakyl radicals are benzyl, alpha-phenylethyl, beta-phenylethyl, alpha-phenylbutyl, and the like.
  • Exemplary cycloalkyl radicals are cyclobutyl, cyclopentyl, cyclohexyl, and the like.
  • Exemplary halogenated hydrocarbon radicals are chloromethyl, bromoethyl, tetrafluorethyl, fluorethyl, trifluorethyl, trifluorotoyl, hexafluoroxylyl, and the like.
  • Viscosity of polysiloxanes useful may vary as widely as the viscosity of polysiloxanes in general vary, so long as the polysiloxane is flowable or can be made to be flowable for application to the tissue paper.
  • the polysiloxane-based oil has an intrinsic viscosity ranging from about 100 to about 1000 centipoises.
  • References disclosing polysiloxanes include U.S. Pat. No. 2,826,551, issued Mar. 11, 1958 to Geen; U.S. Pat. No. 3,964,500, issued Jun. 22, 1976 to Drakoff; U.S. Pat. No. 4,364,837, issued Dec. 21, 1982, Pader, U.S. Pat. No.
  • the present invention is applicable to tissue paper in general, including but not limited to conventionally felt-pressed tissue paper; pattern densified tissue paper such as exemplified in the aforementioned U.S. Patent by Sanford-Sisson and its progeny; and high bulk, uncompacted tissue paper such as exemplified by U.S. Pat. No. 3,812,000, Salvucci, Jr., issued May 21, 1974.
  • the tissue paper may be of a homogenous or multilayered construction; and tissue paper products made therefrom may be of a single-ply or multi-ply construction. Tissue structures formed from layered paper webs are described in U.S. Pat. No. 3,994,771, Morgan, Jr. et al. issued Nov. 30, 1976, U.S. Pat. No.
  • a wet-laid composite, soft, bulky and absorbent paper structure is prepared from two or more layers of furnish which are preferably comprised of different fiber types.
  • the layers are preferably formed from the deposition of separate streams of dilute fiber slurries, the fibers typically being relatively long softwood and relatively short hardwood fibers as used in tissue papermaking, upon one or more endless foraminous screens.
  • the layers are subsequently combined to form a layered composite web.
  • the layered web is subsequently caused to conform to the surface of an open mesh drying/imprinting fabric by the application of a fluid to force to the web and thereafter thermally predried on said fabric as part of a low density papermaking process.
  • the layered web may be stratified with respect to fiber type or the fiber content of the respective layers may be essentially the same.
  • the tissue paper preferably has a basis weight of between 10 g/m 2 and about 65 g/m 2 , and density of about 0.60 g/cc or less.
  • basis weight will be below about 35 g/m 2 or less; and density will be about 0.30 g/cc or less.
  • density will be between 0.04 g/cc and about 0.20 g/cc.
  • Such paper is typically made by depositing papermaking furnish on a foraminous forming wire.
  • This forming wire is often referred to in the art as a Fourdrinier wire.
  • the web is dewatered by pressing the web and drying at elevated temperature.
  • the particular techniques and typical equipment for making webs according to the process just described are well known to those skilled in the art.
  • a low consistency pulp furnish is provided in a pressurized headbox.
  • the headbox has an opening for delivering a thin deposit of pulp furnish onto the Fourdrinier wire to form a wet web.
  • the web is then typically dewatered to a fiber consistency of between about 7% and about 25% (total web weight basis) by vacuum dewatering and further dried by pressing operations wherein the web is subjected to pressure developed by opposing mechanical members, for example, cylindrical rolls.
  • the dewatered web is then further pressed and dried by a steam heated drum apparatus known in the art as a Yankee dryer. Pressure can be developed at the Yankee dryer by mechanical means such as an opposing cylindrical drum pressing against the web. Vacuum may also be applied to the web as it is pressed against the Yankee surface. Multiple Yankee dryer drums may be employed, whereby additional pressing is optionally incurred between the drums.
  • the tissue paper structures which are formed are referred to hereinafter as conventional, pressed, tissue paper structures. Such sheets are considered to be compacted since the web is subjected to substantial overall mechanical compressional forces while the fibers are moist and are then dried (and optionally creped) while in a compressed state.
  • Pattern densifed tissue paper is characterized by having a relatively high bulk field of relatively low fiber density and an array of densified zones of relatively high fiber density.
  • the high bulk field is alternatively characterized as a field of pillow regions.
  • the densified zones are alternatively referred to as knuckle regions.
  • the densified zones may be discretely spaced within the high bulk field or may be interconnected, either fully or partially, within the high bulk field.
  • Preferred processes for making pattern densified tissue webs are disclosed in U.S. Pat. No. 3,301,746, issued to Sanford and Sisson on Jan. 31, 1967, U.S. Pat. No. 3,974,025, issued to Peter G. Ayers on Aug. 10, 1976, and U.S. Pat. No.
  • pattern densifted webs are preferably prepared by depositing a papermaking furnish on a foraminous forming wire such as a Fourdrinier wire to form a wet web and then juxtaposing the web against an array of supports. The web is pressed against the array of supports, thereby resulting in densified zones in the web at the locations geographically corresponding to the points of contact between the array of supports and the wet web. The remainder of the web not compressed during this operation is referred to as the high bulk field.
  • This high bulk field can be further dedensified by application of fluid pressure, such as with a vacuum type device or a blow-through dryer, or by mechanically pressing the web against the array of supports.
  • the web is dewatered, and optionally predried, in such a manner so as to substantially avoid compression of the high bulk field. This is preferably accomplished by fluid pressure, such as with a vacuum type device or blow-through dryer, or alternately by mechanically pressing the web against an array of supports wherein the high bulk field is not compressed.
  • the operations of dewatering, optional predrying and formation of the densifted zones may be integrated or partially integrated to reduce the total number of processing steps performed.
  • the web is dried to completion, preferably still avoiding mechanical pressing.
  • from about 8% to about 55% of the tissue paper surface comprises densifted knuckles having a relative density of at least 125% of the density of the high bulk field.
  • the array of supports is preferably an imprinting carrier fabric having a patterned displacement of knuckles which operate as the array of supports which facilitate the formation of the densifted zones upon application of pressure.
  • the pattern of knuckles constitutes the array of supports previously referred to.
  • Imprinting carrier fabrics are disclosed in U.S. Pat. No. 3,301,746, Sanford and Sisson, issued Jan. 31, 1967, U.S. Pat. No. 3,821,068, Salvucci, Jr. et al., issued May 21, 1974, U.S. Pat. No. 3,974,025, Ayers, issued Aug. 10, 1976, U.S. Pat. No. 3,573,164, Friedberg et al., issued Mar. 30, 1971, U.S. Pat. No.
  • the furnish is first formed into a wet web on a foraminous forming carrier, such as a Fourdrinier wire.
  • the web is dewatered and transferred to an imprinting fabric.
  • the furnish may alternately be initially deposited on a foraminous supporting carrier which also operates as an imprinting fabric.
  • the wet web is dewatered and, preferably, thermally predried to a selected fiber consistency of between about 40% and about 80%.
  • Dewatering can be performed with suction boxes or other vacuum devices or with blow-through dryers.
  • the knuckle imprint of the imprinting fabric is impressed in the web as discussed above, prior to drying the web to completion.
  • One method for accomplishing this is through application of mechanical pressure.
  • nip roll which supports the imprinting fabric against the face of a drying drum, such as a Yankee dryer, wherein the web is disposed between the nip roll and drying drum.
  • the web is molded against the imprinting fabric prior to completion of drying by application of fluid pressure with a vacuum device such as a suction box, or with a blow-through dryer. Fluid pressure may be applied to induce impression of densified zones during initial dewatering, in a separate, subsequent process stage, or a combination thereof.
  • uncompacted, non pattern densified tissue paper structures are prepared by depositing a papermaking furnish and a debonding agent on a foraminous forming wire such as a Fourdrinier wire to form a wet web, draining the web and removing additional water without mechanical compression until the web has a fiber consistency of at least 80%, and creping the web. Water is removed from the web by vacuum dewatering and thermal drying. The resulting structure is a soft but weak high bulk sheet of relatively uncompacted fibers. Bonding material is preferably applied to portions of the web prior to creping.
  • Compacted non-pattern-densified tissue structures are commonly known in the art as conventional tissue structures.
  • compacted, non-pattern-densified tissue paper structures are prepared by depositing a papermaking furnish on a foraminous wire such as a Fourdrinier wire to form a wet web, draining the web and removing additional water with the aid of a uniform mechanical compaction (pressing) until the web has a consistency of 25-50%, transferring the web to a thermal dryer such as a Yankee and creping the web. Overall, water is removed from the web by vacuum, mechanical pressing and thermal means.
  • the resulting structure is strong and generally of singular density, but very low in bulk, absorbency and in softness.
  • tissue paper web of this invention can be used in any application where soft, absorbent tissue paper webs are required.
  • tissue paper web of this invention are in paper towel, toilet tissue and facial tissue products.
  • two tissue paper webs of this invention can be embossed and adhesively secured together in face to face relation as taught by U.S. Pat. No. 3,414,459, which issued to Wells on Dec. 3, 1968 and which is incorporated herein by reference, to form 2-ply paper towels.
  • the papermaking belt 10 travels in the direction indicated by directional arrow B.
  • the papermaking belt 10 passes around the papermaking belt return rolls designated 19a and 19b, impression nip roll 20, papermaking belt return rolls 19c, 19d, 19e and 19f, and emulsion distributing roll 21 (which distributes an emulsion 22 onto the papermaking belt 10 from an emulsion bath 23).
  • emulsion distributing roll 21 which distributes an emulsion 22 onto the papermaking belt 10 from an emulsion bath 23.
  • belt cleaning showers 102 and 102a are belt cleaning showers 102 and 102a, respectively.
  • the purpose of the belt cleaning showers 102 and 102a is to clean the papermaking belt 10 of any paper fibers, adhesives, strength additives, and the like, which remain attached to the section of the papermaking belt 10 after the final step in the papermaking process.
  • the loop that the papermaking belt 10 travels around also includes a means for applying a fluid pressure differential to the paper web, which in the preferred embodiment of the present invention, comprises vacuum pickup shoe 24a and a vacuum box such as multi-slot vacuum box 24.
  • Associated with the papermaking belt 10 of the present invention, and also not shown in FIG. 1 are various additional support rolls, return rolls, cleaning means, drive means, and the like commonly used in papermaking machines and all well known to those skilled in the art.
  • the embryonic web 18 is brought into contact with the papermaking belt 10 of the present invention by the Fourdrinier wire 15 when the Fourdrinier wire 15 is brought near the papermaking belt 10 of the present invention in the vicinity of vacuum pickup shoe 24a.
  • An especially preferred method of continuously applying the polyhydroxy compound and oil to the papermaking belt is via an emulsion distributing roll 21 and emulsion bath 23, illustrated in FIG. 1.
  • the polyhydroxy compound is dissolved into at least one phase of an emulsion 22 comprised of three primary compounds, namely water, oil, and a surfactant, although it is contemplated that other or additional suitable compounds could be used.
  • the emulsion 22 containing the dissolved polyhydroxy compounds and oil is applied to the papermaking belt 10 via the above-mentioned emulsion distributing roll 23.
  • Emulsion 22 can also be applied to the papermaking belt 10 through cleaning showers 102 and 102a.
  • An example of an especially preferred emulsion composition contains water, a petroleum-based oil known as "Regal Oil”, distearyldimethylammonium chloride, cetyl alcohol and a polyhydroxy compound (such as glycerol).
  • distearyldimethylammonium chloride is sold under the trade name ADOGEN TA 100 by the Witco Corporation of Mapleton, Ill.
  • ADOGEN distearyldimethylammonium chloride will be referred to as ADOGEN for convenience.
  • ADOGEN is used in the emulsion as a surfactant to emulsify or stabilize the oil particles (e.g., Regal Oil, Polysiloxane Oil)in the water.
  • release emulsion it is meant that it provides a coating on the papermaking belt 10 so the paper formed releases from (or does not stick to) the same after the steps of the present invention have been performed to the paper web.
  • surfactant refers to a surface active agent, one portion of which is hydrophilic, and another portion of which is hydrophobic, which migrates to the interface between a hydrophilic substance and a hydrophobic substance to stabilize the two substances.
  • cetyl alcohol refers to a C 16 linear fatty alcohol. Cetyl alcohol is manufactured by The Procter & Gamble Company of Cincinnati, Ohio. Cetyl alcohol, like ADOGEN is used as a surfactant in the emulsion utilized in the preferred embodiment of the present invention.
  • the level of polyhydroxy compound and petroleum-based oil or polysiloxane-based oil to be retained by the tissue paper is at least an effective level for imparting a tactile difference in softness or silkiness to the paper.
  • the minimum effective level may vary depending upon the particular type of sheet, the method of application, the particular type of polyhydroxy compound, petroleum-based oil, or polysiloxane-based oil, surfactant, or other additives or treatments.
  • preferably at least about 0.05% of the polyhdroxy compound, and 0.05% of the petroleum-based oil or polysiloxane-based oil is retained by the tissue paper. More preferably, from about 0.1% to about 2.0% of the polyhydroxy compound, and from about 0.1% to about 2.0% of the petroleum-based oil or polysiloxane-based oil is retained by the tissue paper.
  • tissue paper having less than about 0.3% petroleum-based oil or polysiloxane-based oil will provide substantial increases in softness and silkiness yet remain wettable even in the absence of sufficient levels of surfactant to impart a wetting effect.
  • Such paper preferably is treated with surfactant and/or starch as described herein.
  • Tissue paper having in excess of about 0.3% petroleum-based oil or polysiloxane-based oil is preferably treated with a surfactant when contemplated for uses wherein high wettability is desired.
  • the amount of surfactant required to increase hydrophilicity to a desired level will necessarily depend upon the type and level of oil and the type of surfactant. In general, between about 0.1% and about 2.0% surfactant (e.g., Pegosperse®, Igepal®RC-520) retained by the tissue paper is believed to be sufficient to provide sufficiently high wettability for toilet paper and other applications for oil levels less than about 2.0%. However, the benefit of increased wettability is applicable for oil levels well in excess of 2.0%, if a sufficient amount of surfactant is retained by tissue paper.
  • surfactant e.g., Pegosperse®, Igepal®RC-520
  • the level of the polyhydroxy compound retained by the tissue paper can be determined by solvent extraction of the polyhydroxy compound with a solvent.
  • additional procedures may be necessary to remove interfering compounds from the polyhydroxy species of interest.
  • the Weibull solvent extraction method employs a brine solution to isolate polyethylene glycols from nonionic surfactants (Longman, G. F., The Analysis of Detergents and Detergent Products Wiley Interscience, New York, 1975, p. 312). The polyhydroxy species could then be analyzed by spectroscopic or chromatographic techniques.
  • compounds with at least six ethylene oxide units can typically be analyzed spectroscopically by the Ammonium cobaltothiocyanate method (Longman, G. F., The Analysis of Deteraents and Detergent Products, Wiley Interscience, New York, 1975, p. 346). Gas chromatography techniques can also be used to separate and analyze polyhydroxy type compounds. Graphitized poly(2,6-diphenyl-p-phenylene oxide) gas chromatography columns have been used to separate polyethylene glycols with the number of ethylene oxide units ranging from 3 to 9 (Alltech chromatography catalog, number 300, p. 158). The level of polysiloxane-based oil or petroleum-based oil retained by the tissue paper can be determined by solvent extraction of the oil with an organic solvent followed by atomic absorption spectroscopy to determine the level of the oil in the extract
  • the level of nonionic surfactants can be determined by chromatographic techniques.
  • Bruns reported a High Performance Liquid chromatography method with light scattering detection for the analysis of alkyl glycosides (Bruns, A., Waldhoff, H., Winkle, W., Chromatographia, vol. 27, 1989, p. 340).
  • a Supercritical Fluid Chromatography (SFC) technique was also described in the analysis of alkyl glycosides and related species (Lafosse, M., Rollin, P., Elfakir, c., Morin-Allory, L., Martens, M., Dreux, M., Journal of chromatography, vol. 505, 1990, p. 191).
  • the level of anionic surfactants can be determined by water extraction followed by titration of the anionic surfactant in the extract. In some cases, isolation of the linear alkyl sulfonate from interferences may be necessary before the two phase titration analysis (Cross, J., Anionic Surfactants - Chemical Analysis, Dekker, New York, 1977, p. 18, p. 222).
  • the level of starch can be determined by amylase digestion of the starch to glucose followed by colorimetry analysis to determine glucose level. For this starch analysis, background analyses of the paper not containing the starch must be run to subtract out possible contributions made by interfering background species. These methods are exemplary, and are not meant to exclude other methods which may be useful for determining levels of particular components retained by the tissue paper.
  • the paper samples to be tested should be conditioned according to Tappi Method #T402OM-88.
  • samples are preconditioned for 24 hours at a relative humidity level of 10 to 35% and within a temperature range of 22° to 40 ° C.
  • samples should be conditioned for 24 hours at a relative humidity of 48 to 52% and within a temperature range of 22° to 24 ° C.
  • the softness panel testing should take place within the confines of a constant temperature and humidity room. If this is not feasible, all samples, including the controls, should experience identical environmental exposure conditions.
  • Softness testing is performed as a paired comparison in a form similar to that described in "Manual on Sensory Testing Methods", ASTM Special Technical Publication 434, published by the American Society For Testing and Materials 1968 and is incorporated herein by reference. Softness is evaluated by subjective testing using what is referred to as a Paired Difference Test. The method employs a standard external to the test material itself. For tactile perceived softness two samples are presented such that the subject cannot see the samples, and the subject is required to choose one of them on the basis of tactile softness. The result of the test is reported in what is referred to as Panel Score Unit (PSU). With respect to softness testing to obtain the softness data reported herein in PSU, a number of softness panel tests are performed.
  • PSU Panel Score Unit
  • each test ten practiced softness judges are asked to rate the relative softness of three sets of paired samples.
  • the pairs of samples are judged one pair at a time by each judge: one sample of each pair being designated X and the other Y.
  • each X sample is graded against its paired Y sample as follows:
  • a grade of plus one is given if X is judged to may be a little softer than Y, and a grade of minus one is given if Y is judged to may be a little softer than X;
  • a grade of plus two is given if X is judged to surely be a little softer than Y, and a grade of minus two is given if Y is judged to surely be a little softer than X;
  • a grade of plus four is given to X if it is judged to be a whole lot softer than Y, and a grade of minus 4 is given if Y is judged to be a whole lot softer than X.
  • the grades are averaged and the resultant value is in units of PSU.
  • the resulting data are considered the results of one panel test. If more than one sample pair is evaluated then all sample pairs are rank ordered according to their grades by paired statistical analysis. Then, the rank is shifted up or down in value as required to give a zero PSU value to which ever sample is chosen to be the zero-base standard. The other samples then have plus or minus values as determined by their relative grades with respect to the zero base standard.
  • the number of panel tests performed and averaged is such that about 0.2 PSU represents a significant difference in subjectively perceived softness.
  • Hydrophilicity of tissue paper refers, in general, to the propensity of the tissue paper to be wetted with water. Hydrophilicity of tissue paper may be somewhat quantified by determining the period of time required for dry tissue paper to become completely wetted with water. This period of time is referred to as "wetting time". In order to provide a consistent and repeatable test for wetting time, the following procedure may be used for wetting time determinations: first, a conditioned sample unit sheet (the environmental conditions for testing of paper samples are 22° to 24 ° C. and 48 to 52% R. H.
  • tissue paper structure approximately 43/8 inch ⁇ 43/4 inch (about 11.1 cm ⁇ 12 cm) of tissue paper structure is provided; second, the sheet is folded into four (4) juxtaposed quarters, and then crumpled by hand (either covered with clean plastic gloves or copiously washed with a grease removing detergent such as Dawn) into a ball approximately 0.75 inch (about 1.9 cm) to about 1 inch (about 2.5 cm) in diameter; third, the balled sheet is placed on the surface of a body of about 3 liters of distilled water at 22° to 24 ° C. contained in a 3 liter pyrex glass beaker.
  • At least 5 sets of 5 balls should be run for each sample.
  • the final reported result should be the calculated average and standard deviation taken for the 5 sets of data.
  • the units of the measurement are seconds.
  • Another technique to measure the water absorption rate is through pad sink measurements. After conditioning the tissue paper of interest and all controls for a minimum of 24 hours at 22° to 24 ° C. and 48 to 52% relative humidity (Tappi method #T402OM-88), a stack of 5 to 20 sheets of tissue paper is cut to dimensions of 2.5" to 3.0". The cutting can take place through the use of dye cutting presses, a conventional paper cutter, or laser cutting techniques. Manual scissors cutting is not preferred due to both the irreproducibility in handling of the samples, and the potential for paper contamination.
  • This holder is circular in shape and has a diameter of approximately 4.2". It has five straight and evenly spaced metal wires running parallel to one another and across to spot welded points on the wire's circumference. The spacing between the wires is approximately 0.7".
  • This wire mesh screen should be clean and dry prior to placing the paper on its surface.
  • a 3 liter beaker is filled with about 3 liters of distilled water stabilized at a temperature of 22° to 24 ° C. After insuring oneself that the water surface is free of any waves or surface motion, the screen containing the paper is carefully placed on top of the water surface.
  • the screen sample holder is allowed to continue downward after the sample floats on the surface so the sample holder screen handle catches on the side of the beaker. In this way, the screen does not interfere with the water absorption of the paper sample.
  • a timer is started. The timer is stopped after the paper stack is completely wetted out. This is easily visually observed by noting a transition in the paper color from its dry white color to a darker grayish coloration upon complete wetting. At the instant of complete wetting, the timer is stopped and the total time recorded. This total time is the time required for the paper pad to completely wet out.
  • Hydrophilicity characteristics of tissue paper embodiments of the present invention may, of course, be determined immediately after manufacture. However, substantial increases in hydrophobicity may occur during the first two weeks after the tissue paper is made: i.e., after the paper has aged two (2) weeks following its manufacture. Thus, the wetting times are preferably measured at the end of such two week period. Accordingly, wetting times measured at the end of a two week aging period at room temperature are referred to as "two week wetting times.” Also, optional aging conditions of the paper samples may be required to try and mimic both long term storage conditions and/or possible severe temperature and humidity exposures of the paper products of interest. For instance, exposure of the paper sample of interest to temperatures in the range of 49° to 82 ° C.
  • the density of tissue paper is the average density calculated as the basis weight of that paper divided by the caliper, with the appropriate unit conversions incorporated therein to convert to g/cc.
  • Caliper of the tissue paper is the thickness of the preconditioned (23+/-1° C., 50 +/-2% RH for 24 hours according to a TAPPI Method #T4020M-88) paper when subjected to a compressive load of 95 g/in 2 (15.5 g/cm 2 ).
  • the caliper is measured with a Thwing-Albert model 89-11 thickness tester (Thwing-Albert Co. of Philadelphia, Pa.).
  • the basis weight of the paper is typically determined on a 4" ⁇ 4" pad which is 8 plies thick. This pad is preconditioned according to Tappi Method #T402OM-88 and then the weight is measured in units of grams to the nearest ten-thousanths of a gram. Appropriate conversions are made to report the basis weight in units of pounds per 3000 square feet.
  • Dry lint can be measured using a Sutherland Rub Tester, a piece of black felt (made of wool having a thickness of about 2.4 mm and a density of about 0.2 gm/cc. Such felt material is readily available form retail fabric stores such as Hancock Fabric), a four pound weight and a Hunter Color meter.
  • the Sutherland tester is a motor-driven instrument which can stroke a weighted sample back and forth across a stationary sample.
  • the piece of black felt is attached to the four pound weight.
  • the tissue sample is mounted on a piece of cardboard (Crescent #300 obtained from Cordage of Cincinnati, Ohio) The tester then rubs or moves the weighted felt over a stationary tissue sample for five strokes.
  • the load applied to the tissue during rubbing is about 33.1 gm/sq. cm.
  • the Hunter Color L value of the black felt is determined before and after rubbing. The difference in the two Hunter Color readings constitutes a measurement of dry linting. Other methods known in the prior arts for measuring dry lint also can be used.
  • a suitable procedure for measuring the wet linting property of tissue samples is described in U.S. Pat. No. 4,950,545; issued to Walter et al., on Aug. 21, 1990, and incorporated herein by reference.
  • the procedure essentially involves passing a tissue sample through two steel rolls, one of which is partially submerged in a water bath. Lint from the tissue sample is transferred to the steel roll which is moistened by the water bath. The continued rotation of the steel roll deposits the lint into the water bath. The lint is recovered and then counted. See col. 5, line 45-col. 6, line 27 of the Walter et al. patent. Other methods known in the prior art for measuring wet lint also can be used.
  • the present invention may contain as an optional ingredient from about 0.005% to about 3.0%, more preferably from about 0.03% to 1.0% by weight, on a dry fiber basis of a wetting agent.
  • Nonionic Surfactant Alkoxylated Materials
  • Suitable nonionic surfactants can be used as wetting agents in the present invention include addition products of ethylene oxide and, optionally, propylene oxide, with fatty alcohols, fatty acids, fatty amines, etc.
  • Suitable compounds are substantially water-soluble surfactants of the general formula:
  • R 2 for both solid and liquid compositions is selected from the group consisting of primary, secondary and branched chain alkyl and/or acyl hydrocarbyl groups; primary, secondary and branched chain alkenyl hydrocarbyl groups; and primary, secondary and branched chain alkyl- and alkenyl-substituted phenolic hydrocarbyl groups; said hydrocarbyl groups having a hydrocarbyl chain length of from about 8 to about 20, preferably from about 10 to about 18 carbon atoms. More preferably the hydrocarbyl chain length for liquid compositions is from about 16 to about 18 carbon atoms and for solid compositions from about 10 to about 14 carbon atoms.
  • Y is typically --O--, --C(O)O--, --C(O)N(R)--, or --C(O)N(R)R--, in which R 2 , and R, when present, have the meanings given herein before, and/or R can be hydrogen, and z is at least about 8, preferably at least about 10-11. Performance and, usually, stability of the softener composition decrease when fewer ethoxylate groups are present.
  • the nonionic surfactants herein are characterized by an HLB (hydrophiliclipophilic balance) of from about 7 to about 20, preferably from about 8 to about 15.
  • HLB hydrophiliclipophilic balance
  • R 2 and the number of ethoxylate groups the HLB of the surfactant is, in general, determined.
  • the nonionic ethoxylated surfactants useful herein, for concentrated liquid compositions contain relatively long chain R 2 groups and are relatively highly ethoxylated. While shorter alkyl chain surfactants having short ethoxylated groups may possess the requisite HLB, they are not as effective herein.
  • nonionic surfactants follow.
  • the nonionic surfactants of this invention are not limited to these examples.
  • the integer defines the number of ethoxyl (EO) groups in the molecule.
  • deca-, undeca-, dodeca-, tetradeca-, and pentadecaethoxylates of n-hexadecanol, and n-octadecanol having an HLB within the range recited herein are useful wetting agents in the context of this invention.
  • Exemplary ethoxylated primary alcohols useful herein as the viscosity/dispersibility modifiers of the compositions are n--C 18 EO(10); and n--C 10 EO(11).
  • the ethoxylates of mixed natural or synthetic alcohols in the "oleyl" chain length range are also useful herein. Specific examples of such materials include oleylalcohol--EO(11), oleylalcohol--EO(18), and oleylalcohol--EO(25).
  • deca-, undeca-, dodeca-, tetradeca-, pentadeca-, octadeca-, and nonadeca-ethoxylates of 3-hexadecanol, 2-octadecanol, 4-eicosanol, and 5-eicosanol having and HLB within the range recited herein can be used as wetting agents in the present invention.
  • Exemplary ethoxylated secondary alcohols can be used as wetting agents in the present invention are: 2-C 16 EO(11); 2-C 20 EO(11); and 2-C 16 EO(14).
  • the hexa- through octadecaethoxylates of alkylated phenols, particularly monohydric alkylphenols, having an HLB within the range recited herein are useful as the viscosity/dispersibility modifiers of the instant compositions.
  • the hexa- through octadeca-ethoxylates of p-tridecylphenol, m-pentadecylphenol, and the like, are useful herein.
  • Exemplary ethoxylated alkylphenols useful as the wetting agents of the mixtures herein are: p-tridecylphenol EO(11) and p-pentadecylphenol EO(18).
  • a phenylene group in the nonionic formula is the equivalent of an alkylene group containing from 2 to 4 carbon atoms.
  • nonionics containing a phenylene group are considered to contain an equivalent number of carbon atoms calculated as the sum of the carbon atoms in the alkyl group plus about 3.3 carbon atoms for each phenylene group.
  • alkenyl alcohols both primary and secondary, and alkenyl phenols corresponding to those disclosed immediately herein above can be ethoxylated to an HLB within the range recited herein can be used as wetting agents in the present invention
  • Branched chain primary and secondary alcohols which are available from the well-known "OXO" process can be ethoxylated and can be used as wetting agents in the present invention.
  • nonionic surfactant encompasses mixed nonionic surface active agents.
  • the level of surfactant is preferably from about 0.01% to about 2.0% by weight, based on the dry fiber weight of the tissue paper.
  • the surfactants preferably have alkyl chains with eight or more carbon atoms.
  • Exemplary anionic surfactants are linear alkyl sulfonates, and alkylbenzene sulfonates.
  • Exemplary nonionic surfactants are alkylglycosides including alkylglycoside esters such as Crodesta SL-40 which is available from Croda, Inc. (New York, N.Y.); alkylglycoside ethers as described in U.S. Pat. No. 4.011,389, issued to W. K. Langdon, et al. on Mar.
  • alkylpolyethoxylated esters such as Pegosperse 200 ML available from Glyco Chemicals, Inc. (Greenwich, Conn.) and IGEPAL RC-520 available from Rhone Poulenc Corporation (Cranbury, N.J.).
  • the present invention may contain as an optional component an effective amount, preferably from about 0.01% to about 3.0%, more preferably from about 0.2% to about 2.0% by weight, on a dry fiber weight basis, of a water-soluble strength additive resin.
  • strength additive resins are preferably selected from the group consisting of dry strength resins, permanent wet strength resins, temporary wet strength resins, and mixtures thereof.
  • the dry strength additives are preferably selected from the group consisting of carboxymethyl cellulose resins, starch based resins and mixtures thereof.
  • preferred dry strength additives include carboxymethyl cellulose, and cationic polymers from the ACCO chemical family such as ACCO 711 and ACCO 514, with ACCO chemical family being most preferred. These materials are available commercially from the American Cyanamid Company of Wayne, N.J.
  • Permanent wet strength resins useful herein can be of several types. Generally, those resins which have previously found and which will hereafter find utility in the papermaking art are useful herein. Numerous examples are shown in the aforementioned paper by Westfelt, incorporated herein by reference.
  • the wet strength resins are water-soluble, cationic materials. That is to say, the resins are water-soluble at the time they are added to the papermaking furnish. It is quite possible, and even to be expected, that subsequent events such as cross-linking will render the resins insoluble in water. Further, some resins are soluble only under specific conditions, such as over a limited pH range.
  • Wet strength resins are generally believed to undergo a cross-linking or other curing reactions after they have been deposited on, within, or among the papermaking fibers. Cross-linking or curing does not normally occur so long as substantial amounts of water are present.
  • the permanent wet strength resin binder materials are selected from the group consisting of polyamide-epichlorohydrin resins, polyacrylamide resins, and mixtures thereof.
  • Base-activated polyamide-epichlorohydrin resins useful in the present invention are sold under the Santo Res trademark, such as Santo Res 31, by Monsanto Company of St. Louis, Mo. These types of materials are generally described in U.S. Pat. Nos. 3,855,158 issued to Petrovich on Dec. 17, 1974; U.S. Pat. No. 3,899,388 issued to Petrovich on Aug. 12, 1975; U.S. Pat. No. 4,129,528 issued to Petrovich on Dec. 12, 1978; U.S. Pat. No. 4,147,586 issued to Petrovich on Apr. 3, 1979; and U.S. Pat. No. 4,222,921 issued to Van Eenam on Sep. 16, 1980, all incorporated herein by reference.
  • water-soluble cationic resins useful herein are the polyacrylamide resins such as those sold under the Parez trademark, such as Parez 631NC, by American Cyanamid Company of Stanford, Conn. These materials are generally described in U.S. Pat. Nos. 3,556,932 issued to Coscia et al. on Jan. 19, 1971; and U.S. Pat. No. 3,556,933 issued to Williams et al. on Jan. 19, 1971, all incorporated herein by reference.
  • water-soluble resins useful in the present invention include acrylic emulsions and anionic styrene-butadiene latexes. Numerous examples of these types of resins are provided in U.S. Pat. No. 3,844,880, Meisel, Jr. et al., issued Oct. 29, 1974, incorporated herein by reference.
  • Still other water-soluble cationic resins finding utility in this invention are the urea formaldehyde and melamine formaldehyde resins. These polyfunctional, reactive polymers have molecular weights on the order of a few thousand.
  • the more common functional groups include nitrogen containing groups such as amino groups and methylol groups attached to nitrogen.
  • polyethylenimine type resins find utility in the present invention.
  • water-soluble resins include their manufacture, and their manufacture.
  • permanent wet strength resin refers to a resin which allows the paper sheet, when placed in an aqueous medium, to keep a majority of its initial wet strength for a period of time greater than at least two minutes.
  • wet strength additives typically result in paper products with permanent wet strength, i.e., paper which when placed in an aqueous medium retains a substantial portion of its initial wet strength over time.
  • permanent wet strength in some types of paper products can be an unnecessary and undesirable property.
  • Paper products such as toilet tissues, etc., are generally disposed of after brief periods of use into septic systems and the like. Clogging of these systems can result if the paper product permanently retains its hydrolysis-resistant strength properties.
  • manufacturers have added temporary wet strength additives to paper products for which wet strength is sufficient for the intended use, but which then decays upon soaking in water. Decay of the wet strength facilitates flow of the paper product through septic systems.
  • suitable temporary wet strength resins include modified starch temporary wet strength agents, such as National Starch 78-0080, marketed by the National Starch and Chemical Corporation (New York, N.Y.). This type of wet strength agent can be made by reacting dimethoxyethyl-N-methylchloroacetamide with cationic starch polymers. Modified starch temporary wet strength agents are also described in U.S. Pat. No. 4,675,394, Solarek, et al., issued Jun. 23, 1987, and incorporated herein by reference. Preferred temporary wet strength resins include those described in U.S. Pat. No. 4,981,557, Bjorkquist, issued Jan. 1, 1991, and incorporated herein by reference.
  • a pilot scale Fourdrinier papermaking machine is used in the practice of the present invention.
  • a 3% by weight aqueous slurry of NSK Northern Softwood Kraft (such as Grand Prairie from Weyerhaeuser Corporation of Tacoma Wash.)) is made up in a conventional re-pulper.
  • a 2% solution of the temporary wet strength resin i.e., National starch 78-0080 marketed by National Starch and Chemical corporation of New-York, N.Y.
  • the adsorption of the temporary wet strength resin onto NSK fibers is enhanced by an in-line mixer.
  • the NSK slurry is diluted to about 0.2% consistency at the fan pump.
  • a 3% by weight aqueous slurry of Eucalyptus (such as Aracruz of Brazil) fibers is made up in a conventional re-pulper.
  • the Eucalyptus slurry is diluted to about 0.2% consistency at the fan pump.
  • the individual furnish components are sent to separate layers (i.e., Euc. to the outer layers and NSK in the center layer) in the head box and deposited onto a Foudrinier wire to form a three-layer embryonic web. Dewatering occurs through the Fourdrinier wire and is assisted by a deflector and vacuum boxes.
  • the Fourdrinier wire is of a 5-shed, satin weave configuration having 33 machine-direction and 30 cross-machine-direction monofilaments per centimeter, respectively.
  • the embryonic wet web is transferred from the Fourdrinier wire, at a fiber consistency of about 18% at the point of transfer, to a second papermaking belt.
  • the second papermaking belt is an endless belt having the preferred network surface and deflection conduits.
  • the papermaking belt is made by forming a photo-polymeric network on a foraminous woven element made of polyester and having 14 (MD) by 12 (CD) filaments per centimeter in a four shed dual layer design according to the process disclosed in U.S. Pat. No. 5,334,289 issued to Trokhan.
  • the filaments are about 0.22 mm in diameter machine-direction and 0.28 mm in diameter cross-machine-direction.
  • the photosensitive resin used in the process is Merigraph resin EPD1616C, a methacrylated-urethane resin marketed by Hercules, Incorporated, Wilmington, Del.
  • the papermaking belt is about 1.1 mm thick.
  • the embryonic web is carried on the papermaking belt past the vacuum dewatering box, through blow-through predryers after which the web is transferred onto a Yankee dryer.
  • the other process and machine conditions are listed below.
  • the fiber consistency is about 27% after the vacuum dewatering box and, by the action of the predryers, about 65% prior to transfer onto the Yankee dryer; creping adhesive comprising a 0.25% aqueous solution of polyvinyl alcohol is spray applied by applicators; the fiber consistency is increased to be an estimated 99% before dry creping the web with a doctor blade.
  • the doctor blade has a bevel angle of about 25 degrees and is positioned with respect to the Yankee dryer to provide an impact angle of about 81 degrees; the Yankee dryer is operated at about 350° F.
  • the Yankee dryer is operated at about 800 fpm (feet per minute) (about 244 meters per minute).
  • the dry creped web is then passed between two calender rolls.
  • the two calender rolls are biased together at roll weight and operated at surface speeds of 660 fpm (about 201 meters per minute).
  • the calendered web is wound on a reel (which is also operated at a surface speed of 660 fpm) and is then ready for use.
  • aqueous solution containing a plasticizer-emulsion mixture is continuously applied onto the paper-contacting surface of the papermaking belt via an emulsion distribution roll before the papermaking belt comes in contact with the embryonic web.
  • the aqueous emulsion applied by the distribution roll onto the deflection member contains five ingredients: water, Regal Oil (a high-speed turbine oil marketed by the Texaco Oil Company), ADOGEN TA 100 (a distearyldimethyl ammonium chloride surfactant marketed by the Witco Corporation, cetyl alcohol (a C 16 linear fatty alcohol marketed by The Procter & Gamble Company) and glycerol.
  • the relative proportions of the five ingredients are as follows: 6.1% by weight Regal Oil, 0.3% by weight Adogen, 0.2% by weight cetyl alcohol, 31.1% by weight of glycerol, and the remainder water.
  • the emulsion oil phase the emulsion is first mixed with the surfactants listed above, and finally with water and glycerol.
  • the volumetric flow rate of the aqueous emulsion applied to the papermaking belt is about 0.50 gal/hr.-cross-direction ft. (about 6.21 liters/hr-meter).
  • the wet web has a fiber consistency of about 25%, total web weight basis, when it comes in contact with the aqueous emulsion.
  • the web is converted into a one ply tissue paper product.
  • the tissue paper has about 18 #/3M Sq Ft basis weight, contains about 1% of the glycerol, about 1% of the Regal oil and about 0.2% of the temporary wet strength resin.
  • the resulting tissue paper is soft, absorbent and is suitable for use as facial and/or toilet tissues.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Paper (AREA)
  • Sanitary Thin Papers (AREA)
US08/381,250 1995-01-31 1995-01-31 Soft tissue paper containing an oil and a polyhydroxy compound Expired - Lifetime US5575891A (en)

Priority Applications (16)

Application Number Priority Date Filing Date Title
US08/381,250 US5575891A (en) 1995-01-31 1995-01-31 Soft tissue paper containing an oil and a polyhydroxy compound
KR1019970705182A KR100249609B1 (ko) 1995-01-31 1996-01-22 오일과 폴리하이드록시 화합물을 함유하는 부드러운 티슈지
JP52429596A JP3939345B2 (ja) 1995-01-31 1996-01-22 油及びポリヒドロキシ化合物に含有する柔らかいティッシュペーパー
CN96191681A CN1075576C (zh) 1995-01-31 1996-01-22 含油和多羟基化合物的柔软薄页纸
DE69608542T DE69608542T3 (de) 1995-01-31 1996-01-22 Öl und polyhydroxyverbindung enthaltendes weiches tissue-papier
AU49059/96A AU713070B2 (en) 1995-01-31 1996-01-22 Soft tissue paper containing an oil and a polyhydroxy compound
BR9607084A BR9607084A (pt) 1995-01-31 1996-01-22 Papel de seda
PCT/US1996/001145 WO1996024719A2 (en) 1995-01-31 1996-01-22 Soft tissue paper containing an oil and a polyhydroxy compound
AT96905250T ATE193349T1 (de) 1995-01-31 1996-01-22 Öl und polyhydroxyverbindung enthaltendes weiches tissue-papier
EP96905250A EP0807194B2 (en) 1995-01-31 1996-01-22 Soft tissue paper containing an oil and a polyhydroxy compound
CA002208643A CA2208643C (en) 1995-01-31 1996-01-22 Soft tissue paper containing an oil and a polyhydroxy compound
ES96905250T ES2145998T3 (es) 1995-01-31 1996-01-22 Papel tisu suave que contiene un aceite y un compuesto polihidroxilado.
ZA96700A ZA96700B (en) 1995-01-31 1996-01-30 Soft tissue paper containing an oil and a polyhydroxy compound
TW085101212A TW402653B (en) 1995-01-31 1996-01-31 Soft tissue paper containing an oil and a polyhydroxy compound
MXPA/A/1997/005778A MXPA97005778A (en) 1995-01-31 1997-07-30 Soft hygienic paper containing an oil and a polyhidrox compound
HK98103946A HK1004681A1 (en) 1995-01-31 1998-05-07 Soft tissue paper containing an oil and a polyhydroxy compound

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US08/381,250 US5575891A (en) 1995-01-31 1995-01-31 Soft tissue paper containing an oil and a polyhydroxy compound

Publications (1)

Publication Number Publication Date
US5575891A true US5575891A (en) 1996-11-19

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Country Status (15)

Country Link
US (1) US5575891A (ko)
EP (1) EP0807194B2 (ko)
JP (1) JP3939345B2 (ko)
KR (1) KR100249609B1 (ko)
CN (1) CN1075576C (ko)
AT (1) ATE193349T1 (ko)
AU (1) AU713070B2 (ko)
BR (1) BR9607084A (ko)
CA (1) CA2208643C (ko)
DE (1) DE69608542T3 (ko)
ES (1) ES2145998T3 (ko)
HK (1) HK1004681A1 (ko)
TW (1) TW402653B (ko)
WO (1) WO1996024719A2 (ko)
ZA (1) ZA96700B (ko)

Cited By (76)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5782963A (en) 1996-03-29 1998-07-21 Kimberly-Clark Worldwide, Inc. Colorant stabilizers
US5814190A (en) * 1994-06-29 1998-09-29 The Procter & Gamble Company Method for making paper web having both bulk and smoothness
US5855655A (en) 1996-03-29 1999-01-05 Kimberly-Clark Worldwide, Inc. Colorant stabilizers
US5858586A (en) 1993-08-05 1999-01-12 Kimberly-Clark Corporation Digital information recording media and method of using same
US5882478A (en) * 1997-11-12 1999-03-16 Kimberly-Clark Worldwide, Inc. Tissue products containing esters of polyoxyethylene alkyl ether carboxylic acids
US5885337A (en) 1995-11-28 1999-03-23 Nohr; Ronald Sinclair Colorant stabilizers
US5891229A (en) 1996-03-29 1999-04-06 Kimberly-Clark Worldwide, Inc. Colorant stabilizers
US5908495A (en) 1993-08-05 1999-06-01 Nohr; Ronald Sinclair Ink for ink jet printers
US5935384A (en) * 1995-12-06 1999-08-10 Kawano Paper Co. Ltd Water-disintegrable paper having moisture retaining property and process for producing the same
US6001218A (en) 1994-06-29 1999-12-14 Kimberly-Clark Worldwide, Inc. Production of soft paper products from old newspaper
US6008268A (en) 1994-10-21 1999-12-28 Kimberly-Clark Worldwide, Inc. Photoreactor composition, method of generating a reactive species, and applications therefor
US6017471A (en) 1993-08-05 2000-01-25 Kimberly-Clark Worldwide, Inc. Colorants and colorant modifiers
US6017661A (en) 1994-11-09 2000-01-25 Kimberly-Clark Corporation Temporary marking using photoerasable colorants
US6027610A (en) 1994-06-29 2000-02-22 Kimberly-Clark Corporation Production of soft paper products from old newspaper
US6033465A (en) 1995-06-28 2000-03-07 Kimberly-Clark Worldwide, Inc. Colorants and colorant modifiers
US6060200A (en) 1993-08-05 2000-05-09 Kimberly-Clark Worldwide, Inc. Photo-erasable data processing forms and methods
US6063551A (en) 1995-06-05 2000-05-16 Kimberly-Clark Worldwide, Inc. Mutable dye composition and method of developing a color
US6071979A (en) 1994-06-30 2000-06-06 Kimberly-Clark Worldwide, Inc. Photoreactor composition method of generating a reactive species and applications therefor
US6074527A (en) 1994-06-29 2000-06-13 Kimberly-Clark Worldwide, Inc. Production of soft paper products from coarse cellulosic fibers
US6090236A (en) 1994-06-30 2000-07-18 Kimberly-Clark Worldwide, Inc. Photocuring, articles made by photocuring, and compositions for use in photocuring
US6096152A (en) * 1997-04-30 2000-08-01 Kimberly-Clark Worldwide, Inc. Creped tissue product having a low friction surface and improved wet strength
US6099628A (en) 1996-03-29 2000-08-08 Kimberly-Clark Worldwide, Inc. Colorant stabilizers
WO2000055423A1 (en) * 1999-03-12 2000-09-21 Metso Paper, Inc. Method and apparatus for handling a paper or board web
US6174412B1 (en) 1998-03-02 2001-01-16 Purely Cotton, Inc. Cotton linter tissue products and method for preparing same
US6187695B1 (en) 1998-12-08 2001-02-13 Kimberly-Clark Worldwide, Inc. Cool feeling tissue product and method
US6211383B1 (en) 1993-08-05 2001-04-03 Kimberly-Clark Worldwide, Inc. Nohr-McDonald elimination reaction
WO2001029312A1 (en) * 1999-10-15 2001-04-26 Hercules Incorporated Process combining functional additives and dryer section passivation
US6228157B1 (en) 1998-07-20 2001-05-08 Ronald S. Nohr Ink jet ink compositions
US6242057B1 (en) 1994-06-30 2001-06-05 Kimberly-Clark Worldwide, Inc. Photoreactor composition and applications therefor
US6265458B1 (en) 1998-09-28 2001-07-24 Kimberly-Clark Worldwide, Inc. Photoinitiators and applications therefor
US6277897B1 (en) 1998-06-03 2001-08-21 Kimberly-Clark Worldwide, Inc. Photoinitiators and applications therefor
US6294698B1 (en) 1999-04-16 2001-09-25 Kimberly-Clark Worldwide, Inc. Photoinitiators and applications therefor
US6331056B1 (en) 1999-02-25 2001-12-18 Kimberly-Clark Worldwide, Inc. Printing apparatus and applications therefor
US6344109B1 (en) 1998-12-18 2002-02-05 Bki Holding Corporation Softened comminution pulp
US6368396B1 (en) 1999-01-19 2002-04-09 Kimberly-Clark Worldwide, Inc. Colorants, colorant stabilizers, ink compositions, and improved methods of making the same
US6368395B1 (en) 1999-05-24 2002-04-09 Kimberly-Clark Worldwide, Inc. Subphthalocyanine colorants, ink compositions, and method of making the same
US6387210B1 (en) 1998-09-30 2002-05-14 Kimberly-Clark Worldwide, Inc. Method of making sanitary paper product from coarse fibers
US6398911B1 (en) 2000-01-21 2002-06-04 Kimberly-Clark Worldwide, Inc. Modified polysaccharides containing polysiloxane moieties
US6416624B1 (en) 1997-10-10 2002-07-09 Union Carbide Chemicals & Plastics Technology Corporation Spray application of an additive composition to sheet materials
US6420013B1 (en) * 1996-06-14 2002-07-16 The Procter & Gamble Company Multiply tissue paper
US6432270B1 (en) 2001-02-20 2002-08-13 Kimberly-Clark Worldwide, Inc. Soft absorbent tissue
US6465602B2 (en) 2000-01-20 2002-10-15 Kimberly-Clark Worldwide, Inc. Modified condensation polymers having azetidinium groups and containing polysiloxane moieties
US6464830B1 (en) 2000-11-07 2002-10-15 Kimberly-Clark Worldwide, Inc. Method for forming a multi-layered paper web
US6503559B1 (en) 1998-06-03 2003-01-07 Kimberly-Clark Worldwide, Inc. Neonanoplasts and microemulsion technology for inks and ink jet printing
US6511580B1 (en) 2001-11-15 2003-01-28 Kimberly-Clark Worldwide, Inc. Soft absorbent tissue containing derivitized amino-functional polysiloxanes
US6511579B1 (en) 1998-06-12 2003-01-28 Fort James Corporation Method of making a paper web having a high internal void volume of secondary fibers and a product made by the process
US6514383B1 (en) 2001-11-15 2003-02-04 Kimberly-Clark Worldwide, Inc. Soft absorbent tissue containing derivitized amino-functional polysiloxanes
US6517678B1 (en) 2000-01-20 2003-02-11 Kimberly-Clark Worldwide, Inc. Modified polysaccharides containing amphiphillic hydrocarbon moieties
US6524379B2 (en) 1997-08-15 2003-02-25 Kimberly-Clark Worldwide, Inc. Colorants, colorant stabilizers, ink compositions, and improved methods of making the same
US6576087B1 (en) 2001-11-15 2003-06-10 Kimberly-Clark Worldwide, Inc. Soft absorbent tissue containing polysiloxanes
US6582558B1 (en) 2001-11-15 2003-06-24 Kimberly-Clark Worldwide, Inc. Soft absorbent tissue containing hydrophilic polysiloxanes
WO2003057987A2 (en) * 2001-12-31 2003-07-17 Kimberly-Clark Worldwide, Inc. Method for reducing bad smells in paper
US6596126B1 (en) 1999-01-25 2003-07-22 Kimberly-Clark Worldwide, Inc. Modified polysaccharides containing aliphatic hydrocarbon moieties
US6599393B1 (en) 2001-11-15 2003-07-29 Kimberly-Clark Worldwide, Inc. Soft absorbent tissue containing hydrophilically-modified amino-functional polysiloxanes
US20030155089A1 (en) * 2001-12-31 2003-08-21 Kimberly-Clark Worldwide, Inc. Process for manufacturing a cellulosic paper product exhibiting reduced malodor
US20040045687A1 (en) * 2002-09-11 2004-03-11 Shannon Thomas Gerard Method for using water insoluble chemical additives with pulp and products made by said method
US6749721B2 (en) 2000-12-22 2004-06-15 Kimberly-Clark Worldwide, Inc. Process for incorporating poorly substantive paper modifying agents into a paper sheet via wet end addition
US20040237210A1 (en) * 2001-06-20 2004-12-02 Thomas Thoroe-Scherb Method and an apparatus for the manufacture of a fiber web provided with a three-dimensional surface structure
US6896769B2 (en) 1999-01-25 2005-05-24 Kimberly-Clark Worldwide, Inc. Modified condensation polymers containing azetidinium groups in conjunction with amphiphilic hydrocarbon moieties
US6916402B2 (en) 2002-12-23 2005-07-12 Kimberly-Clark Worldwide, Inc. Process for bonding chemical additives on to substrates containing cellulosic materials and products thereof
US20060124261A1 (en) * 2003-09-02 2006-06-15 Lindsay Jeffrey D Method of making a clothlike pattern densified web
US20060275347A1 (en) * 2005-06-03 2006-12-07 The Procter & Gamble Company Fibrous structures comprising a polymer structure
US7297231B2 (en) 2004-07-15 2007-11-20 Kimberly-Clark Worldwide, Inc. Binders curable at room temperature with low blocking
CN100422441C (zh) * 2001-03-07 2008-10-01 金伯利-克拉克环球公司 用水不溶性化学添加剂处理纸浆的方法
US7449085B2 (en) 2003-09-02 2008-11-11 Kimberly-Clark Worldwide, Inc. Paper sheet having high absorbent capacity and delayed wet-out
US20090188636A1 (en) * 2008-01-28 2009-07-30 Salaam Latisha Evette Soft tissue paper having a polyhydroxy compound applied onto a surface thereof
US20090188637A1 (en) * 2008-01-28 2009-07-30 Eric Chan Soft tissue paper having a polyhydroxy compound and lotion applied onto a surface thereof
US7670459B2 (en) 2004-12-29 2010-03-02 Kimberly-Clark Worldwide, Inc. Soft and durable tissue products containing a softening agent
US20100096096A1 (en) * 2007-04-30 2010-04-22 Jose Luis Egiburu Use of an additive for the production of decorative paper
US20100143584A1 (en) * 2006-10-26 2010-06-10 Kou-Chang Liu Method of Making Soft and Absorbent Tissue Products
US7749355B2 (en) * 2005-09-16 2010-07-06 The Procter & Gamble Company Tissue paper
US20110217345A1 (en) * 2008-07-22 2011-09-08 Fuming Huang Emulsion composition, methods of softening fibrous structures using the same, and fibrous substrate treated therewith
US8147649B1 (en) 2006-06-15 2012-04-03 Clearwater Specialties Llc Creping adhesive modifier and methods for producing paper products
WO2022006287A1 (en) * 2020-06-30 2022-01-06 Kemira Oyj Methods for measuring dust and lint
US11274398B2 (en) * 2018-02-28 2022-03-15 Daio Paper Corporation Tissue paper
US11280050B2 (en) * 2018-02-28 2022-03-22 Daio Paper Corporation Tissue paper

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5624532A (en) * 1995-02-15 1997-04-29 The Procter & Gamble Company Method for enhancing the bulk softness of tissue paper and product therefrom
JP3297340B2 (ja) * 1997-02-13 2002-07-02 河野製紙株式会社 紙製品
US6860967B2 (en) 2001-01-19 2005-03-01 Sca Hygiene Products Gmbh Tissue paper penetrated with softening lotion
US6905697B2 (en) 2001-01-19 2005-06-14 Sca Hygiene Products Gmbh Lotioned fibrous web having a short water absorption time
US20040253890A1 (en) * 2003-06-13 2004-12-16 Ostgard Estelle Anne Fibers with lower edgewise compression strength and sap containing composites made from the same
JP3860815B2 (ja) * 2004-01-30 2006-12-20 大王製紙株式会社 クレープ紙の製造方法およびクレープ紙
DE102006050324A1 (de) 2006-10-25 2008-04-30 Sca Hygiene Products Gmbh Tissuepapierprodukt mit einer Seidenproteine enthaltenden Lotion
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US8101045B2 (en) * 2010-01-05 2012-01-24 Nalco Company Modifying agent for yankee coatings
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AU2019293273A1 (en) * 2018-06-28 2021-01-21 Kimberly-Clark Worldwide, Inc. Lotion treated tissue product
JP7090858B1 (ja) * 2021-10-22 2022-06-27 河野製紙株式会社 繊維ウェブ製品及びその製造方法
JP7036307B1 (ja) * 2021-10-22 2022-03-15 河野製紙株式会社 繊維ウェブ製品及びその製造方法

Citations (41)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2683087A (en) * 1948-02-10 1954-07-06 American Cyanamid Co Absorbent cellulosic products
US2683088A (en) * 1952-06-10 1954-07-06 American Cyanamid Co Soft bibulous sheet
US3014832A (en) * 1957-02-12 1961-12-26 Kimberly Clark Co Method of fabricating tissue
US3301746A (en) * 1964-04-13 1967-01-31 Procter & Gamble Process for forming absorbent paper by imprinting a fabric knuckle pattern thereon prior to drying and paper thereof
US3554863A (en) * 1968-06-25 1971-01-12 Riegel Textile Corp Cellulose fiber pulp sheet impregnated with a long chain cationic debonding agent
US3755220A (en) * 1971-10-13 1973-08-28 Scott Paper Co Cellulosic sheet material having a thermosetting resin bonder and a surfactant debonder and method for producing same
US3844880A (en) * 1971-01-21 1974-10-29 Scott Paper Co Sequential addition of a cationic debonder, resin and deposition aid to a cellulosic fibrous slurry
US3974025A (en) * 1974-04-01 1976-08-10 The Procter & Gamble Company Absorbent paper having imprinted thereon a semi-twill, fabric knuckle pattern prior to final drying
US3994771A (en) * 1975-05-30 1976-11-30 The Procter & Gamble Company Process for forming a layered paper web having improved bulk, tactile impression and absorbency and paper thereof
US4144122A (en) * 1976-10-22 1979-03-13 Berol Kemi Ab Quaternary ammonium compounds and treatment of cellulose pulp and paper therewith
US4191609A (en) * 1979-03-09 1980-03-04 The Procter & Gamble Company Soft absorbent imprinted paper sheet and method of manufacture thereof
US4300981A (en) * 1979-11-13 1981-11-17 The Procter & Gamble Company Layered paper having a soft and smooth velutinous surface, and method of making such paper
US4351699A (en) * 1980-10-15 1982-09-28 The Procter & Gamble Company Soft, absorbent tissue paper
US4377543A (en) * 1981-10-13 1983-03-22 Kimberly-Clark Corporation Strength and softness control of dry formed sheets
US4441962A (en) * 1980-10-15 1984-04-10 The Procter & Gamble Company Soft, absorbent tissue paper
US4447294A (en) * 1981-12-30 1984-05-08 The Procter & Gamble Company Process for making absorbent tissue paper with high wet strength and low dry strength
US4529480A (en) * 1983-08-23 1985-07-16 The Procter & Gamble Company Tissue paper
US4637859A (en) * 1983-08-23 1987-01-20 The Procter & Gamble Company Tissue paper
US4795530A (en) * 1985-11-05 1989-01-03 Kimberly-Clark Corporation Process for making soft, strong cellulosic sheet and products made thereby
US4940513A (en) * 1988-12-05 1990-07-10 The Procter & Gamble Company Process for preparing soft tissue paper treated with noncationic surfactant
US4950545A (en) * 1989-02-24 1990-08-21 Kimberly-Clark Corporation Multifunctional facial tissue
US4959125A (en) * 1988-12-05 1990-09-25 The Procter & Gamble Company Soft tissue paper containing noncationic surfactant
US5059282A (en) * 1988-06-14 1991-10-22 The Procter & Gamble Company Soft tissue paper
JPH04100995A (ja) * 1990-08-10 1992-04-02 Nippon Oil & Fats Co Ltd 紙用柔軟剤組成物
US5164046A (en) * 1989-01-19 1992-11-17 The Procter & Gamble Company Method for making soft tissue paper using polysiloxane compound
US5215626A (en) * 1991-07-19 1993-06-01 The Procter & Gamble Company Process for applying a polysiloxane to tissue paper
US5217576A (en) * 1991-11-01 1993-06-08 Dean Van Phan Soft absorbent tissue paper with high temporary wet strength
US5223096A (en) * 1991-11-01 1993-06-29 Procter & Gamble Company Soft absorbent tissue paper with high permanent wet strength
US5227242A (en) * 1989-02-24 1993-07-13 Kimberly-Clark Corporation Multifunctional facial tissue
US5240562A (en) * 1992-10-27 1993-08-31 Procter & Gamble Company Paper products containing a chemical softening composition
US5246546A (en) * 1992-08-27 1993-09-21 Procter & Gamble Company Process for applying a thin film containing polysiloxane to tissue paper
US5246545A (en) * 1992-08-27 1993-09-21 Procter & Gamble Company Process for applying chemical papermaking additives from a thin film to tissue paper
US5262007A (en) * 1992-04-09 1993-11-16 Procter & Gamble Company Soft absorbent tissue paper containing a biodegradable quaternized amine-ester softening compound and a temporary wet strength resin
US5264082A (en) * 1992-04-09 1993-11-23 Procter & Gamble Company Soft absorbent tissue paper containing a biodegradable quaternized amine-ester softening compound and a permanent wet strength resin
US5279767A (en) * 1992-10-27 1994-01-18 The Procter & Gamble Company Chemical softening composition useful in fibrous cellulosic materials
US5312522A (en) * 1993-01-14 1994-05-17 Procter & Gamble Company Paper products containing a biodegradable chemical softening composition
US5334286A (en) * 1993-05-13 1994-08-02 The Procter & Gamble Company Tissue paper treated with tri-component biodegradable softener composition
US5385643A (en) * 1994-03-10 1995-01-31 The Procter & Gamble Company Process for applying a thin film containing low levels of a functional-polysiloxane and a nonfunctional-polysiloxane to tissue paper
US5385642A (en) * 1993-05-13 1995-01-31 The Procter & Gamble Company Process for treating tissue paper with tri-component biodegradable softener composition
US5389204A (en) * 1994-03-10 1995-02-14 The Procter & Gamble Company Process for applying a thin film containing low levels of a functional-polysiloxane and a mineral oil to tissue paper
US5405501A (en) * 1993-06-30 1995-04-11 The Procter & Gamble Company Multi-layered tissue paper web comprising chemical softening compositions and binder materials and process for making the same

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3818533A (en) * 1969-07-18 1974-06-25 Alustikin Prod Inc Treated paper and non-woven material for wiping surfaces and method therefor
WO1989001072A1 (en) * 1987-07-24 1989-02-09 Paper Chemistry Laboratory, Inc. Method for manufacture of paper products
CA2155222C (en) * 1990-06-29 1997-11-11 Paul Dennis Trokhan Process for making absorbent paper web
JP2996319B2 (ja) † 1991-12-03 1999-12-27 河野製紙株式会社 高水分含有性を有するティッシュペーパー
US5449551A (en) * 1993-06-03 1995-09-12 Kawano Paper Co., Ltd. Highly water absorbent fibrous web and a process for producing the same
AU1295895A (en) † 1993-12-13 1995-07-03 Procter & Gamble Company, The Lotion composition for imparting soft, lubricious feel to tissue paper

Patent Citations (41)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2683087A (en) * 1948-02-10 1954-07-06 American Cyanamid Co Absorbent cellulosic products
US2683088A (en) * 1952-06-10 1954-07-06 American Cyanamid Co Soft bibulous sheet
US3014832A (en) * 1957-02-12 1961-12-26 Kimberly Clark Co Method of fabricating tissue
US3301746A (en) * 1964-04-13 1967-01-31 Procter & Gamble Process for forming absorbent paper by imprinting a fabric knuckle pattern thereon prior to drying and paper thereof
US3554863A (en) * 1968-06-25 1971-01-12 Riegel Textile Corp Cellulose fiber pulp sheet impregnated with a long chain cationic debonding agent
US3844880A (en) * 1971-01-21 1974-10-29 Scott Paper Co Sequential addition of a cationic debonder, resin and deposition aid to a cellulosic fibrous slurry
US3755220A (en) * 1971-10-13 1973-08-28 Scott Paper Co Cellulosic sheet material having a thermosetting resin bonder and a surfactant debonder and method for producing same
US3974025A (en) * 1974-04-01 1976-08-10 The Procter & Gamble Company Absorbent paper having imprinted thereon a semi-twill, fabric knuckle pattern prior to final drying
US3994771A (en) * 1975-05-30 1976-11-30 The Procter & Gamble Company Process for forming a layered paper web having improved bulk, tactile impression and absorbency and paper thereof
US4144122A (en) * 1976-10-22 1979-03-13 Berol Kemi Ab Quaternary ammonium compounds and treatment of cellulose pulp and paper therewith
US4191609A (en) * 1979-03-09 1980-03-04 The Procter & Gamble Company Soft absorbent imprinted paper sheet and method of manufacture thereof
US4300981A (en) * 1979-11-13 1981-11-17 The Procter & Gamble Company Layered paper having a soft and smooth velutinous surface, and method of making such paper
US4351699A (en) * 1980-10-15 1982-09-28 The Procter & Gamble Company Soft, absorbent tissue paper
US4441962A (en) * 1980-10-15 1984-04-10 The Procter & Gamble Company Soft, absorbent tissue paper
US4377543A (en) * 1981-10-13 1983-03-22 Kimberly-Clark Corporation Strength and softness control of dry formed sheets
US4447294A (en) * 1981-12-30 1984-05-08 The Procter & Gamble Company Process for making absorbent tissue paper with high wet strength and low dry strength
US4529480A (en) * 1983-08-23 1985-07-16 The Procter & Gamble Company Tissue paper
US4637859A (en) * 1983-08-23 1987-01-20 The Procter & Gamble Company Tissue paper
US4795530A (en) * 1985-11-05 1989-01-03 Kimberly-Clark Corporation Process for making soft, strong cellulosic sheet and products made thereby
US5059282A (en) * 1988-06-14 1991-10-22 The Procter & Gamble Company Soft tissue paper
US4940513A (en) * 1988-12-05 1990-07-10 The Procter & Gamble Company Process for preparing soft tissue paper treated with noncationic surfactant
US4959125A (en) * 1988-12-05 1990-09-25 The Procter & Gamble Company Soft tissue paper containing noncationic surfactant
US5164046A (en) * 1989-01-19 1992-11-17 The Procter & Gamble Company Method for making soft tissue paper using polysiloxane compound
US4950545A (en) * 1989-02-24 1990-08-21 Kimberly-Clark Corporation Multifunctional facial tissue
US5227242A (en) * 1989-02-24 1993-07-13 Kimberly-Clark Corporation Multifunctional facial tissue
JPH04100995A (ja) * 1990-08-10 1992-04-02 Nippon Oil & Fats Co Ltd 紙用柔軟剤組成物
US5215626A (en) * 1991-07-19 1993-06-01 The Procter & Gamble Company Process for applying a polysiloxane to tissue paper
US5217576A (en) * 1991-11-01 1993-06-08 Dean Van Phan Soft absorbent tissue paper with high temporary wet strength
US5223096A (en) * 1991-11-01 1993-06-29 Procter & Gamble Company Soft absorbent tissue paper with high permanent wet strength
US5262007A (en) * 1992-04-09 1993-11-16 Procter & Gamble Company Soft absorbent tissue paper containing a biodegradable quaternized amine-ester softening compound and a temporary wet strength resin
US5264082A (en) * 1992-04-09 1993-11-23 Procter & Gamble Company Soft absorbent tissue paper containing a biodegradable quaternized amine-ester softening compound and a permanent wet strength resin
US5246546A (en) * 1992-08-27 1993-09-21 Procter & Gamble Company Process for applying a thin film containing polysiloxane to tissue paper
US5246545A (en) * 1992-08-27 1993-09-21 Procter & Gamble Company Process for applying chemical papermaking additives from a thin film to tissue paper
US5240562A (en) * 1992-10-27 1993-08-31 Procter & Gamble Company Paper products containing a chemical softening composition
US5279767A (en) * 1992-10-27 1994-01-18 The Procter & Gamble Company Chemical softening composition useful in fibrous cellulosic materials
US5312522A (en) * 1993-01-14 1994-05-17 Procter & Gamble Company Paper products containing a biodegradable chemical softening composition
US5334286A (en) * 1993-05-13 1994-08-02 The Procter & Gamble Company Tissue paper treated with tri-component biodegradable softener composition
US5385642A (en) * 1993-05-13 1995-01-31 The Procter & Gamble Company Process for treating tissue paper with tri-component biodegradable softener composition
US5405501A (en) * 1993-06-30 1995-04-11 The Procter & Gamble Company Multi-layered tissue paper web comprising chemical softening compositions and binder materials and process for making the same
US5385643A (en) * 1994-03-10 1995-01-31 The Procter & Gamble Company Process for applying a thin film containing low levels of a functional-polysiloxane and a nonfunctional-polysiloxane to tissue paper
US5389204A (en) * 1994-03-10 1995-02-14 The Procter & Gamble Company Process for applying a thin film containing low levels of a functional-polysiloxane and a mineral oil to tissue paper

Non-Patent Citations (9)

* Cited by examiner, † Cited by third party
Title
U.S. Appl. 08/004,333 Phan et al. Jan. 14, 1993. *
U.S. Appl. 08/072,297 Phan et al. Jun. 3, 1993. *
U.S. Appl. 08/072,299 Laughlin et al. Jun. 3, 1993. *
U.S. Appl. 08/085,852 Phan et al. Jun. 30, 1993. *
U.S. Appl. 08/140,571 Phan et al. Oct. 22, 1993. *
U.S. Appl. 08/141,320 Phan et al. Oct. 22, 1993. *
U.S. Appl. 08/308,896 Phan et al. Sep. 20, 1994. *
U.S. Appl. 08/309,993 Phan et al. Sep. 20, 1994. *
U.S. Appl. 08/359,124 Ampulski et al. Dec. 19, 1994. *

Cited By (114)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6017471A (en) 1993-08-05 2000-01-25 Kimberly-Clark Worldwide, Inc. Colorants and colorant modifiers
US6211383B1 (en) 1993-08-05 2001-04-03 Kimberly-Clark Worldwide, Inc. Nohr-McDonald elimination reaction
US5858586A (en) 1993-08-05 1999-01-12 Kimberly-Clark Corporation Digital information recording media and method of using same
US6127073A (en) 1993-08-05 2000-10-03 Kimberly-Clark Worldwide, Inc. Method for concealing information and document for securely communicating concealed information
US6120949A (en) 1993-08-05 2000-09-19 Kimberly-Clark Worldwide, Inc. Photoerasable paint and method for using photoerasable paint
US6066439A (en) 1993-08-05 2000-05-23 Kimberly-Clark Worldwide, Inc. Instrument for photoerasable marking
US5908495A (en) 1993-08-05 1999-06-01 Nohr; Ronald Sinclair Ink for ink jet printers
US6060200A (en) 1993-08-05 2000-05-09 Kimberly-Clark Worldwide, Inc. Photo-erasable data processing forms and methods
US6060223A (en) 1993-08-05 2000-05-09 Kimberly-Clark Worldwide, Inc. Plastic article for colored printing and method for printing on a colored plastic article
US6054256A (en) 1993-08-05 2000-04-25 Kimberly-Clark Worldwide, Inc. Method and apparatus for indicating ultraviolet light exposure
US6342305B1 (en) 1993-09-10 2002-01-29 Kimberly-Clark Corporation Colorants and colorant modifiers
US6001218A (en) 1994-06-29 1999-12-14 Kimberly-Clark Worldwide, Inc. Production of soft paper products from old newspaper
US6027610A (en) 1994-06-29 2000-02-22 Kimberly-Clark Corporation Production of soft paper products from old newspaper
US5814190A (en) * 1994-06-29 1998-09-29 The Procter & Gamble Company Method for making paper web having both bulk and smoothness
US6074527A (en) 1994-06-29 2000-06-13 Kimberly-Clark Worldwide, Inc. Production of soft paper products from coarse cellulosic fibers
US6071979A (en) 1994-06-30 2000-06-06 Kimberly-Clark Worldwide, Inc. Photoreactor composition method of generating a reactive species and applications therefor
US6090236A (en) 1994-06-30 2000-07-18 Kimberly-Clark Worldwide, Inc. Photocuring, articles made by photocuring, and compositions for use in photocuring
US6242057B1 (en) 1994-06-30 2001-06-05 Kimberly-Clark Worldwide, Inc. Photoreactor composition and applications therefor
US6008268A (en) 1994-10-21 1999-12-28 Kimberly-Clark Worldwide, Inc. Photoreactor composition, method of generating a reactive species, and applications therefor
US6017661A (en) 1994-11-09 2000-01-25 Kimberly-Clark Corporation Temporary marking using photoerasable colorants
US6235095B1 (en) 1994-12-20 2001-05-22 Ronald Sinclair Nohr Ink for inkjet printers
US6063551A (en) 1995-06-05 2000-05-16 Kimberly-Clark Worldwide, Inc. Mutable dye composition and method of developing a color
US6033465A (en) 1995-06-28 2000-03-07 Kimberly-Clark Worldwide, Inc. Colorants and colorant modifiers
US6168655B1 (en) 1995-11-28 2001-01-02 Kimberly-Clark Worldwide, Inc. Colorant stabilizers
US5885337A (en) 1995-11-28 1999-03-23 Nohr; Ronald Sinclair Colorant stabilizers
US5935384A (en) * 1995-12-06 1999-08-10 Kawano Paper Co. Ltd Water-disintegrable paper having moisture retaining property and process for producing the same
US6099628A (en) 1996-03-29 2000-08-08 Kimberly-Clark Worldwide, Inc. Colorant stabilizers
US6168654B1 (en) 1996-03-29 2001-01-02 Kimberly-Clark Worldwide, Inc. Colorant stabilizers
US5782963A (en) 1996-03-29 1998-07-21 Kimberly-Clark Worldwide, Inc. Colorant stabilizers
US5855655A (en) 1996-03-29 1999-01-05 Kimberly-Clark Worldwide, Inc. Colorant stabilizers
US5891229A (en) 1996-03-29 1999-04-06 Kimberly-Clark Worldwide, Inc. Colorant stabilizers
US6420013B1 (en) * 1996-06-14 2002-07-16 The Procter & Gamble Company Multiply tissue paper
US6096152A (en) * 1997-04-30 2000-08-01 Kimberly-Clark Worldwide, Inc. Creped tissue product having a low friction surface and improved wet strength
US6524379B2 (en) 1997-08-15 2003-02-25 Kimberly-Clark Worldwide, Inc. Colorants, colorant stabilizers, ink compositions, and improved methods of making the same
US6416624B1 (en) 1997-10-10 2002-07-09 Union Carbide Chemicals & Plastics Technology Corporation Spray application of an additive composition to sheet materials
US5882478A (en) * 1997-11-12 1999-03-16 Kimberly-Clark Worldwide, Inc. Tissue products containing esters of polyoxyethylene alkyl ether carboxylic acids
US6174412B1 (en) 1998-03-02 2001-01-16 Purely Cotton, Inc. Cotton linter tissue products and method for preparing same
US6503559B1 (en) 1998-06-03 2003-01-07 Kimberly-Clark Worldwide, Inc. Neonanoplasts and microemulsion technology for inks and ink jet printing
US6277897B1 (en) 1998-06-03 2001-08-21 Kimberly-Clark Worldwide, Inc. Photoinitiators and applications therefor
US20050103455A1 (en) * 1998-06-12 2005-05-19 Fort James Corporation Method of making a paper web having a high internal void volume of secondary fibers
US20100314059A1 (en) * 1998-06-12 2010-12-16 Georgia-Pacific Consumer Products Lp Method of making a paper web having a high internal void volume of secondary fibers
US7794566B2 (en) 1998-06-12 2010-09-14 Georgia-Pacific Consumer Products Lp Method of making a paper web having a high internal void volume of secondary fibers
US6824648B2 (en) 1998-06-12 2004-11-30 Fort James Corporation Method of making a paper web having a high internal void volume of secondary fibers and a product made by the process
US6511579B1 (en) 1998-06-12 2003-01-28 Fort James Corporation Method of making a paper web having a high internal void volume of secondary fibers and a product made by the process
US20030136531A1 (en) * 1998-06-12 2003-07-24 Fort James Corporation Method of making a paper web having a high internal void volume of secondary fibers and a product made by the process
US8366881B2 (en) 1998-06-12 2013-02-05 Georgia-Pacific Consumer Products Lp Method of making a paper web having a high internal void volume of secondary fibers
US6228157B1 (en) 1998-07-20 2001-05-08 Ronald S. Nohr Ink jet ink compositions
US6265458B1 (en) 1998-09-28 2001-07-24 Kimberly-Clark Worldwide, Inc. Photoinitiators and applications therefor
US6387210B1 (en) 1998-09-30 2002-05-14 Kimberly-Clark Worldwide, Inc. Method of making sanitary paper product from coarse fibers
US6187695B1 (en) 1998-12-08 2001-02-13 Kimberly-Clark Worldwide, Inc. Cool feeling tissue product and method
US6533898B2 (en) 1998-12-18 2003-03-18 Bki Holding Corporation Softened comminution pulp
US6344109B1 (en) 1998-12-18 2002-02-05 Bki Holding Corporation Softened comminution pulp
US6368396B1 (en) 1999-01-19 2002-04-09 Kimberly-Clark Worldwide, Inc. Colorants, colorant stabilizers, ink compositions, and improved methods of making the same
US6620295B2 (en) 1999-01-25 2003-09-16 Kimberly-Clark Worldwide, Inc. Modified polysaccharides containing amphiphilic hydrocarbon moieties
US6896769B2 (en) 1999-01-25 2005-05-24 Kimberly-Clark Worldwide, Inc. Modified condensation polymers containing azetidinium groups in conjunction with amphiphilic hydrocarbon moieties
US6596126B1 (en) 1999-01-25 2003-07-22 Kimberly-Clark Worldwide, Inc. Modified polysaccharides containing aliphatic hydrocarbon moieties
US6331056B1 (en) 1999-02-25 2001-12-18 Kimberly-Clark Worldwide, Inc. Printing apparatus and applications therefor
WO2000055423A1 (en) * 1999-03-12 2000-09-21 Metso Paper, Inc. Method and apparatus for handling a paper or board web
US6994771B1 (en) 1999-03-12 2006-02-07 Metso Paper, Inc. Method and apparatus for handling a paper or board web
US6294698B1 (en) 1999-04-16 2001-09-25 Kimberly-Clark Worldwide, Inc. Photoinitiators and applications therefor
US6368395B1 (en) 1999-05-24 2002-04-09 Kimberly-Clark Worldwide, Inc. Subphthalocyanine colorants, ink compositions, and method of making the same
WO2001029312A1 (en) * 1999-10-15 2001-04-26 Hercules Incorporated Process combining functional additives and dryer section passivation
US6517678B1 (en) 2000-01-20 2003-02-11 Kimberly-Clark Worldwide, Inc. Modified polysaccharides containing amphiphillic hydrocarbon moieties
US6465602B2 (en) 2000-01-20 2002-10-15 Kimberly-Clark Worldwide, Inc. Modified condensation polymers having azetidinium groups and containing polysiloxane moieties
US6398911B1 (en) 2000-01-21 2002-06-04 Kimberly-Clark Worldwide, Inc. Modified polysaccharides containing polysiloxane moieties
US6464830B1 (en) 2000-11-07 2002-10-15 Kimberly-Clark Worldwide, Inc. Method for forming a multi-layered paper web
US7678232B2 (en) 2000-12-22 2010-03-16 Kimberly-Clark Worldwide, Inc. Process for incorporating poorly substantive paper modifying agents into a paper sheet via wet end addition
US6749721B2 (en) 2000-12-22 2004-06-15 Kimberly-Clark Worldwide, Inc. Process for incorporating poorly substantive paper modifying agents into a paper sheet via wet end addition
US6432270B1 (en) 2001-02-20 2002-08-13 Kimberly-Clark Worldwide, Inc. Soft absorbent tissue
CN100422441C (zh) * 2001-03-07 2008-10-01 金伯利-克拉克环球公司 用水不溶性化学添加剂处理纸浆的方法
US20040237210A1 (en) * 2001-06-20 2004-12-02 Thomas Thoroe-Scherb Method and an apparatus for the manufacture of a fiber web provided with a three-dimensional surface structure
US7291249B2 (en) * 2001-06-20 2007-11-06 Voith Paper Patent Gmbh Apparatus for the manufacture of a structured fiber web
US6511580B1 (en) 2001-11-15 2003-01-28 Kimberly-Clark Worldwide, Inc. Soft absorbent tissue containing derivitized amino-functional polysiloxanes
US6514383B1 (en) 2001-11-15 2003-02-04 Kimberly-Clark Worldwide, Inc. Soft absorbent tissue containing derivitized amino-functional polysiloxanes
US6582558B1 (en) 2001-11-15 2003-06-24 Kimberly-Clark Worldwide, Inc. Soft absorbent tissue containing hydrophilic polysiloxanes
US6599393B1 (en) 2001-11-15 2003-07-29 Kimberly-Clark Worldwide, Inc. Soft absorbent tissue containing hydrophilically-modified amino-functional polysiloxanes
US6576087B1 (en) 2001-11-15 2003-06-10 Kimberly-Clark Worldwide, Inc. Soft absorbent tissue containing polysiloxanes
US7297228B2 (en) 2001-12-31 2007-11-20 Kimberly-Clark Worldwide, Inc. Process for manufacturing a cellulosic paper product exhibiting reduced malodor
WO2003057987A2 (en) * 2001-12-31 2003-07-17 Kimberly-Clark Worldwide, Inc. Method for reducing bad smells in paper
US20030155089A1 (en) * 2001-12-31 2003-08-21 Kimberly-Clark Worldwide, Inc. Process for manufacturing a cellulosic paper product exhibiting reduced malodor
WO2003057987A3 (en) * 2001-12-31 2003-12-04 Kimberly Clark Co Method for reducing bad smells in paper
US7229530B2 (en) 2001-12-31 2007-06-12 Kimberly-Clark Worldwide, Inc. Method for reducing undesirable odors generated by paper hand towels
US20030145965A1 (en) * 2001-12-31 2003-08-07 Kimberly-Clark Worldwide, Inc. Method for reducing undesirable odors generated by paper hand towels
US20040045687A1 (en) * 2002-09-11 2004-03-11 Shannon Thomas Gerard Method for using water insoluble chemical additives with pulp and products made by said method
WO2004025029A1 (en) * 2002-09-11 2004-03-25 Kimberly-Clark Worldwide, Inc. Improved method for using water insoluble chemical additives with pulp and products made by said method
US6916402B2 (en) 2002-12-23 2005-07-12 Kimberly-Clark Worldwide, Inc. Process for bonding chemical additives on to substrates containing cellulosic materials and products thereof
US20060124261A1 (en) * 2003-09-02 2006-06-15 Lindsay Jeffrey D Method of making a clothlike pattern densified web
US7435312B2 (en) * 2003-09-02 2008-10-14 Kimberly-Clark Worldwide, Inc. Method of making a clothlike pattern densified web
US7449085B2 (en) 2003-09-02 2008-11-11 Kimberly-Clark Worldwide, Inc. Paper sheet having high absorbent capacity and delayed wet-out
US7678856B2 (en) 2004-07-15 2010-03-16 Kimberly-Clark Worldwide Inc. Binders curable at room temperature with low blocking
US7678228B2 (en) 2004-07-15 2010-03-16 Kimberly-Clark Worldwide, Inc. Binders curable at room temperature with low blocking
US7297231B2 (en) 2004-07-15 2007-11-20 Kimberly-Clark Worldwide, Inc. Binders curable at room temperature with low blocking
US7670459B2 (en) 2004-12-29 2010-03-02 Kimberly-Clark Worldwide, Inc. Soft and durable tissue products containing a softening agent
US20090260746A1 (en) * 2005-06-03 2009-10-22 Linda Evers Smith Process for making fibrous structures comprising a polymer structure
US9103056B2 (en) 2005-06-03 2015-08-11 The Procter & Gamble Company Fibrous structures comprising a polymer structure
US7572504B2 (en) * 2005-06-03 2009-08-11 The Procter + Gamble Company Fibrous structures comprising a polymer structure
US7615278B2 (en) 2005-06-03 2009-11-10 The Proctor & Gamble Company Fibrous structures comprising a polymer structure
US8535466B2 (en) 2005-06-03 2013-09-17 The Procter & Gamble Company Process for making fibrous structures comprising a polymer structure
US20060275347A1 (en) * 2005-06-03 2006-12-07 The Procter & Gamble Company Fibrous structures comprising a polymer structure
US7749355B2 (en) * 2005-09-16 2010-07-06 The Procter & Gamble Company Tissue paper
US8147649B1 (en) 2006-06-15 2012-04-03 Clearwater Specialties Llc Creping adhesive modifier and methods for producing paper products
US8608904B1 (en) 2006-06-15 2013-12-17 Clearwater Specialties, LLC Creping adhesive modifier and methods for producing paper products
US20100143584A1 (en) * 2006-10-26 2010-06-10 Kou-Chang Liu Method of Making Soft and Absorbent Tissue Products
US20100096096A1 (en) * 2007-04-30 2010-04-22 Jose Luis Egiburu Use of an additive for the production of decorative paper
US8070913B2 (en) 2008-01-28 2011-12-06 The Procter & Gamble Company Soft tissue paper having a polyhydroxy compound applied onto a surface thereof
US8187419B2 (en) 2008-01-28 2012-05-29 The Procter & Gamble Company Soft tissue paper having a polyhydroxy compound and lotion applied onto a surface thereof
US7972475B2 (en) * 2008-01-28 2011-07-05 The Procter & Gamble Company Soft tissue paper having a polyhydroxy compound and lotion applied onto a surface thereof
US7867361B2 (en) * 2008-01-28 2011-01-11 The Procter & Gamble Company Soft tissue paper having a polyhydroxy compound applied onto a surface thereof
US20090188636A1 (en) * 2008-01-28 2009-07-30 Salaam Latisha Evette Soft tissue paper having a polyhydroxy compound applied onto a surface thereof
US20090188637A1 (en) * 2008-01-28 2009-07-30 Eric Chan Soft tissue paper having a polyhydroxy compound and lotion applied onto a surface thereof
US20110217345A1 (en) * 2008-07-22 2011-09-08 Fuming Huang Emulsion composition, methods of softening fibrous structures using the same, and fibrous substrate treated therewith
US11274398B2 (en) * 2018-02-28 2022-03-15 Daio Paper Corporation Tissue paper
US11280050B2 (en) * 2018-02-28 2022-03-22 Daio Paper Corporation Tissue paper
WO2022006287A1 (en) * 2020-06-30 2022-01-06 Kemira Oyj Methods for measuring dust and lint

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